职责
The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH 良好临床实践: 综合指南,” (地面控制点), supporting client programs administrated by Watermark ensure project data and summary statements are of known and documented quality.
要求
Will be expected to travel extensively to study sites in the US to monitor our clinical and outcome studies.
Successful applicant must have previous experience monitoring clinical trials.
全球监管要求和/或药物开发实践的基本知识.
了解/理解监管机构的方法和观点.
基本技能和能力
良好的书面和口头沟通能力, demonstrated ability to function effectively with all levels of management
强大的谈判和建立关系的能力
Good understanding of medical / corporate governance principles
Detailed oriented and organized
0 条评论